Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs61271866
rs61271866
1 1.000 0.080 9 21997016 intron variant T/A snv 0.19 0.700 1.000 1 2014 2014
dbSNP: rs1063192
rs1063192
24 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs1333049
rs1333049
60 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2019 2019
dbSNP: rs2151280
rs2151280
16 0.701 0.360 9 22034720 non coding transcript exon variant G/A snv 0.46 0.010 < 0.001 1 2015 2015
dbSNP: rs2157719
rs2157719
17 0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 0.010 1.000 1 2014 2014
dbSNP: rs564398
rs564398
18 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 0.010 1.000 1 2013 2013
dbSNP: rs573687
rs573687
3 0.882 0.120 9 22011643 intron variant G/A snv 0.26 0.010 1.000 1 2013 2013
dbSNP: rs615552
rs615552
4 0.925 0.120 9 22026078 intron variant T/C snv 0.29 0.010 1.000 1 2013 2013